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Huber Needle

EUDAMED

Class IIa (EU MDR)

Ref HN3 202502 O

by Know Medical Srl

Identity

Trade Name
HUBER NEEDLE EUDAMED
Device Name
HUBER NEEDLE - Ago di Huber 20Gx25mm con prolunga e Y EUDAMED
Model / Reference
HN3 202502 O EUDAMED

Identifiers

Primary DI / UDI-DI
08049033192865 EUDAMED
Basic UDI-DI
B-08049033192865 EUDAMED
EMDN Code
A01010302 NEEDLES AND KITS FOR IMPLANTABLE SYSTEMS (PORT), W/O SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Huber Needle by Know Medical Srl — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Know Medical Srl
EUDAMED SRN
IT-MF-000013457

Sources (1)

  • EUDAMED fa2654bc-62d3-4bc2-8522-f3933bf3988e 61 fields · synced Jun 18, 2026